EUA
OMNIgene·ORAL OM-505 and OME-505 (OMNIgene·ORAL) saliva collection devices
FDA Emergency Use Authorization · DNA Genotek Inc. · Oct 28, 2020
Key facts
| Product | OMNIgene·ORAL OM-505 and OME-505 (OMNIgene·ORAL) saliva collection devices |
|---|---|
| Company | DNA Genotek Inc. |
| Product type | Saliva Collection Device |
| Date | Oct 28, 2020 |
| FDA page | fda.gov |
At a glance
- 1–9 Authorization documents
- 1–9 EUAs for this company
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Emergency Use Authorizations
Emergency Use Authorizations allow the FDA to permit unapproved medical products, or unapproved uses of approved products, during a declared public health emergency.
Source: U.S. Food and Drug Administration (FDA), Emergency Use Authorizations · Source date: